Medical sling procedures and anchor insertion methods and devices

ABSTRACT

A procedure for treating urinary stress incontinence by using bone anchors, whether screw or staple type, with or without suture, inserted pervaginaily for use with a sling material for supporting the bladder neck and/or proximal urethra.

RELATED APPLICATIONS

[0001] The present application claims the priority of U.S. patentapplication No. 08/733,798, filed Oct. 18, 1996 (pending; the priorityof U.S. patent application No. 08/622,598 filed Mar. 26, 1996 (patented,and issued as U.S. Pat. No. 5,807,403 on Sep. 15, 1998); the priority ofU.S. patent application No. 08/150,517 filed on Nov. 10, 1993 (patented,and issued as U.S. Pat.No. 5,520,700 on May 28, 1996); the priority ofIsraeli Patent application No. 103737, filed Nov. 13, 1992; the priorityof U.S. provisional application No. 60/012,205, filed Feb. 23, 1996; andthe priority of U.S. provisional patent application No. 60/005,348,filed Oct. 18, 1995; and the priority of Israeli Patent application No.127978, filed Jan. 8, 1999. The present application claims all domesticand foreign priority benefits of these prior applications, all of whichare fully incorporated herein by reference.

FIELD OF THE INVENTION

[0002] The present invention relates to pervaginal sling proceduresusing bone anchors.

BACKGROUND OF THE INVENTION AND DESCRIPTION OF THE PRIOR ARTS

[0003] Urinary stress incontinence, i.e., the inability to controlurination from the bladder, is a distressing problem for more than tenpercent of elderly women as well as for many young women. Differenttheories exist to explain the pathology. In a normally anatomicallypositioned bladder, the proximal urethra and the bladder are in pressurecontinuity with the abdominal cavity, so that an increase in abdominalpressure is transmitted both to the bladder and to the proximal urethra,resulting in normal continence. However, particularly among elderlywomen, the bladder and the proximal urethra tend to descend from theirnormal or original anatomic positions such that the bladder neck andproximal urethra move away from the posterior wall of the pubic bone.When this occurs, the proximal urethra is no longer in pressurecontinuity with the abdominal cavity; therefore, an unintended increasein intraabdominal pressure (e.g. by laughing or coughing results in anincrease in intravesical pressure, but no change in the urethral closingpressure, thereby producing so-called stress incontinence. It alsoappears that as the bladder descends, the urethra becomes shorter andcurved, so that its radial tonic muscle contraction is reduced,contributing to incontinence. Another pathology may arise from urethralsphincteric damage (type III incontinence).

[0004] Most of the surgical treatments for stress incontinence involvebladder neck suspension. One treatment is by an open surgical operation,involving an incision in the abdominal wall and/or anterior vaginalwall, to reposition and suspend the bladder and proximal urethra totheir normal or original anatomic positions. This is done by suspensionof the bladder neck and periurethral tissue to the posterior wall of thepubic bone. In another surgical procedure, the bladder neck is elevatedby suspension of suture threads passing, with the aid of long needles,from both sides of the urethra and the bladder neck to the lowerabdominal fascia or superior pubic bone ramus.

[0005] In prior U.S. patents and applications (e.g., the RelatedApplications referenced above, including U.S. Pat. No. 5,520,700, issuedMay 28, 1996, pending U.S. patent application Ser. No. 08/733,798, filedOct. 18, 1996, and pending Israeli Patent Application Serial No. 127978,filed Jan. 8, 1999 and entitled “Incontinence Device”, the disclosuresof which are hereby incorporated by reference), apparatus and methodsare disclosed which allow treatment of urinary stress incontinence by apervaginal procedure. As disclosed therein, an inserter device can beutilized for ejecting and implanting a bone anchor (e.g. a staple or abone screw) through the vaginal tissue to enter the pubic bone. Further,a non-linear inserter device can be used to install a bone anchor byeither injecting Cn the case of a staple) or screwing the bone screwinto the pubic bone, with or without vaginal incision. The suture threadthat is secured to the bone anchor(s) (e.g staple(s) or bone screw(s)),can be used to suspend the bladder neck and the periurethral tissue tothe posterior wall of the pubic bone. In addition, the suture thread canbe used to perform a sling procedure in which a piece of material, suchas abdominal fascia, fascia lata, cadaveric fascia or syntheticmaterial, is positioned below the bladder neck and attached at bothextremities to the pubic bone, by the threads. (In the classic slingoperation, the sling material is attached to the abdominal fascia eitherdirectly or by means of threads).

[0006] It has been found, however, in stapler devices, and especiallythose that require high impact for bone implantation, that the ejectionof the staple from the device causes the stapler to recoil. As isapparent from basic physics, the action of ejecting the staple from thestapler is associated with a reaction force which forces theinserter/stapler and the hand of the individual (the physician)implanting the same to move backwards. As a result, the physician musttake this recoil into account and use force to firmly press the stapleragainst the pubic bone to ensure that the bone anchor is properly andeffectively ejected and implanted. Anyone familiar with carpentry-typestaple guns is familiar with this recoil. If pressure is not placed overthe head end of the stapler, and the surface into which the staple isdriven is hard (as in the case of bone), the staple will not be fullyimplanted, but, rather, the user's hand will recoil. The medical staplershould also be held perpendicular to the bone surface. The stapler mustbe held in that position with the stapler held firmly during and throughthe ejection process so that the stapler does not shift its position asa result of the recoil. Otherwise, undue movement of the stapler becauseof recoil can result in a staple being ejected in an incorrectorientation, or incompletely ejected into the bone of the patient. Thisproblem is especially apparent where the material into which the stapleis ejected is bone and the physical confines of the space where themedical physician's hands are working is limited, i.e., within a vagina.

[0007] Similarly, where the inserter is a screwdriver type and theanchor is a screw type anchor, unless a hole is pre-drilled in theinsertion site, constant firm pressure must be applied through the axisof the anchor (perpendicular to the pubic bone) to assist theself-tapping property of the anchor to facilitate insertion duringscrewing. The medical screwdriver type inserter must, therefore, be heldin the correct position relative to the patient's anatomy through theinsertion process.

[0008] A purpose of the present invention is to provide mechanicalleverage, which facilitates a constant pressure at the insertion site tominimize the effect of this recoil, increasing the ease of use of aninserter device in a medical procedure (whether a pusher or impact typeinserter, or a screw inserter), and increasing an inserter device'seffectiveness. This furthers the selftapping property of the boneanchor, whether it be an impact type or screw type anchor. A screw typeinserter device can be used for greater ease and effectiveness of useover an impact type device, particularly in a pervaginal medicalprocedure.

[0009] A further purpose of the present invention is to provide leveragein the per vaginal insertion of a bone anchor into the pubic bone. Thepresent invention allows the physician to employ a pulling forceperpendicularly against the pubic bone of the patient, and toconveniently do so with one hand. The leverage, degree of accuracy andease of insertion are believed to be significantly enhanced by thepresent invention.

[0010] In one embodiment, the present invention relates to per vaginalbone screw or staple insertion, without first drilling a hole in thebone, by use of a non-linear or C-shaped inserter having a rotatingintravaginal head for per vaginal injecting or screwing with or withoutvaginal wall incision. An additional purpose of the present invention isto provide a screw or staple type bone anchor and related device andprocedures for per vaginal incisionless or minimal incision bladder necksuspension.

[0011] In a further embodiment, the invention relates to medical slingprocedures. It is believed by some physicians that a sling procedure hasbetter long term results of bladder neck suspension for type I, II, andIII incontinence. Therefore, the invention relates, in a furtherembodiment, to medical sling procedures using bone anchors, eitherstaples or screws, with or without suture, and preferably further usinga non-linear anchor inserter.

[0012] Such sling procedures (or “sling operations”) are medicalprocedures in which a sling material is positioned below the bladderneck and/or the urethra to give support like a hammock. Sling procedureshave been described in the art in such references as: Blavias J G,Jacobs B Z, Pubovaginal fascial sling for the treatment of complicatedstress urinary incontinence, J. Urol. 145(6):1214-8 (Jun. 1991); McGuireE J, Lytton B, Pubovaginal sling procedure for stress incontinence, J.Urol. 119(1):82-4 (Jan. 1978); and, McGuire E J, Abdominal procedure forstress incontinence, Urol. Clin. North Am., 12(2):285-90 (May 1985); thedisclosures of which are incorporated herein by reference.

[0013] In these relatively rninimally invasive techniques (which haverecently become more common), the bladder neck and/or urethra issupported by a sling, so that the urethra is partially compressed and/orhas a support below it. Thus, during straining and/or bladder/uretheraldescent, pressure is applied between the urethra and the sling, therebyclosing its lumen.

[0014] Benderev et. al, in U.S. Pat. No. 5,836,314 and Brenneman et al,in PCT publication WO 98/19606, the disclosures of which is incorporatedherein by reference, describe examples of procedures for treatingincontinence. Two or more bone anchors are attached to the pubic bone,and each anchor is pre-threaded with a suture. Brenneman suggests that asling be attached to the sutures and that the the sutures then be pulledtight and knotted, thereby urging the sling towards the pubic bone.Benderev suggests integrally molding one end of a suture with a “suturesupport”, which suture support is provided to prevent damage to theurethra by the sutures.

SUMMARY OF THE INVENTION

[0015] An object of the present invention is to provide a stapler devicewhich is particularly useful for fastening threaded staples to a bonefor various medical purposes, particularly to treat urinary stressincontinence.

[0016] According to one embodiment of the present invention, there isprovided a stapler device comprising: a handle manually grippable by auser, containing a drive mechanism and a trigger to activate the drivemechanism; a barrel fixed to the handle; a guide for holding a staple tobe ejected; and an ejector driven by the drive mechanism, movable in thebarrel for ejecting a staple out through an end of the guide;characterized in that the end of the guide is formed to accommodate asuture thread fixed to the staple.

[0017] In one described embodiment, the barrel is rigid for holding theguide in a fixed prescribed direction; and in a second describedembodiment, it is flexible to allow pointing of the guide in a desireddirection.

[0018] In a third described embodiment, the end of the guide is formedwith a slot, or a pair of slots, for receiving the thread fixed to thestaple; and in a fourth described embodiment, it is formed with arecess, or a pair of recesses, for receiving the thread fixed to thestaple.

[0019] Such an anchoring device is particularly useful for treatingwomen suffering from urinary stress incontinence caused by thedescending of the bladder and the proximal urethra from their normalanatomical positions. Thus, the anchor may be ejected through thevaginal wall to enter the pubic bone, and the suture thread secured tothe anchor may be used for attaching the bladder neck and the proximalurethra to the posterior wall of the pubic bone. Such an anchor devicemay also be used in other applications; for example, in medicaloperations for the fixation of a shoulder capsule in a person sufferingfrom chronic shoulder dislocation.

[0020] The present invention also addresses the difficulties experiencedin the prior art by providing a “C”, “V” or other non-linear snapedinsertion device for use in medical applications, and especially, pervaginal insertions of anchors of any type into the pubic bone of apatient. The insertion device, which may be rigid or flexible, ispositioned during use so that force may be applied through the axis ofthe anchor. The weight of a patient can contribute to the force appliedby the physician to firmly press the device against the patient'sanatomy, so as to minimize the effects of the problems normallyassociated with recoil. The present device is directed both toward astapler device for use to eject a staple type bone anchor, and toward ascrew type bone anchor inserter. The inserters can be useful in otherapplications, as well, beyond those applications disclosed herein.

[0021] Accordingly, it is an object of the present invention to providean insertion device which minimizes recoil during ejection of a boneanchor into bone.

[0022] It is further an object of the present invention to provide aninsertion device which minimizes recoil during per vaginal insertion ofa bone anchor into the pubic bone and otherwise allows constant pressureto be applied during the per vaginal insertion of self-tapping anchorsinto the pubic bone.

[0023] It is a further object of the present invention to provide adevice which facilitates additional pressure to be applied to theinsertion site beyond the direct pushing pressure applied by thephysician in the case of a linear inserter held in place in the vaginaby the physician's hand. With the present non-linear inserter, thephysician's hand is used to pull the inserter against the resistiveforce of the pubic bone, thereby forcing the anchor tip to penetrate thebone cortex. It is far easier to insert a bone anchor, staple or screwwith the hands external to the vagina and by use of the pulling forceperpendicular to the bone surface.

[0024] It is further an object of the present invention to provide aninserter device for medical applications which improves the accuracy,effectiveness and ease of anchor insertions.

[0025] It is further an object of the present invention to utilize thephysical pulling force on the inserter to further fixate the anchor tippenetration force perpendicular to the bone surface and in line with thephysician pulling force.

[0026] It is further an object of the present invention to utilize atleast a portion of the weight of a patient's body to maintain a boneanchor or screw inserter in firm contact with the patient duringinsertion of a bone anchor or screw into the patient's bone.

[0027] It is a further object of the present invention to use at least aportion of the weight of a patient as counter balancing leverage againstthe recoil of a bone anchor/staple/screw being inserted into the bone ofa patient.

[0028] It is further an object of tile present invention to provideimproved procedures and inserter devices for inserting bone anchors,staples and/or screws in medical procedures.

[0029] It is further an object of the present invention to provide animproved bone anchor inserter for use in and to facilitate medicalapplications.

[0030] It is further an object of the present invention to provideimproved bone anchors and bone anchor inserters.

[0031] It is further an object of the present invention to provideimproved bone anchors and bone anchor inserters for treatment of femaleurinary stress incontinence and for other medical applications.

[0032] It is further an object of the present invention to provideimproved methods for treatment of urinary stress incontinence.

[0033] It is further an object of the present invention to provideimproved methods for treatment of urinary stress incontinence includingper vaginal bone anchor insertion into the pubic bone. These boneanchors are preferably either in the form of staples or screws. The boneanchor inserter has either a non-linear (e.g. a “C”or “V” shape) or alinear shape and is operated either by an impact or by a rotationalmovement to insert a staple or screw into the bone with or withoutvaginal wall incision.

[0034] It is further an object of the present invention to provideimproved methods for treatment of urinary stress incontinence by pervaginal bone anchor insertion into the pubic bone.

[0035] It is further an object of the present invention to provideimproved methods for treatment of urinary stress incontinence by pervaginal bone anchor insertion into the pubic bone and the use of a slingprocedure.

[0036] It is further an object of the present invention to provideimproved methods for treatment of urinary stress incontinence by thesuspension of the bladder neck by pervaginal bone anchor insertion intothe pubic bone and the use of a nonlinear inserter and a slingprocedure.

[0037] It is further an object of the present invention to provideimproved methods for treatment of urinary stress incontinence by pervaginal suspension of a sling from the pubic bone.

[0038] The invention also provides bone anchors, such as staples andscrews, having suture thread secured thereto, for ejection by boneanchor insertion devices, including, but not limited to, those describedherein, and for use in accordance with medical procedures.

[0039] Further features and advantages of the invention will be apparentin conjunction wih the description and the drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

[0040] The invention is herein described, by way of example only, withreference to the accompanying figures, wherein:

[0041]FIG. 1 illustrates one form of a bone anchor inserter deviceconstructed in accordance with the present invention.

[0042]FIGS. 2 and 3 illustrate the natural curved shape and thetemporary straight shape respectively, of one form of staple withattached thread in accordance with the present invention.

[0043]FIG. 4 is an enlarged sectional view of the staple guide in thebone anchor inserter device of FIG. 1.

[0044]FIG. 5a is an end view illustrating the staple guide of FIG. 4;FIG. 5b is similar to FIG. 5a, illustrating a modification in theconstruction of the staple guide.

[0045]FIGS. 6, 7a, and 7 b are views similar to FIGS. 4, 5a, and 5 b,respectively, illustrating a modification in the construction of thestaple guide.

[0046]FIG. 8 illustrates various stages in applying the staple andthread of FIGS. 2 and 3 to the pubic bone when a procedure for treatingurinary stress incontinence is performed (or for insertion into otherbone when treating other conditions).

[0047] FIGS. 9-11 illustrate modifications in the construction of thebone anchor inserter device of FIG. 1.

[0048]FIG. 12a is a left side view of a stapler or pusher/impact typebone anchor inserter, in accordance with the present invention, with afront view of a loading key shown as well.

[0049]FIG. 12b is a bottom, back, and left side perspective view (on adifferent scale) of the stapler or pusher/impact type bone anchorinserter of FIG. 12a.

[0050]FIG. 12c is a right cross-sectional view of a screwdriver-typebone anchor inserter for rotational insertion of bone screws.

[0051]FIGS. 12d(1)-12 d(6) are front views of bone screws for use in thescrewdriver-type bone anchor inserter of FIG. 12c. Several differentbone screw embodiments are shown, in accordance with the presentinvention.

[0052]FIG. 12e is a right cross-sectional view of a spring loadedC-shaped inserter, having an alternative driving mechanism, a springmechanism.

[0053] FIGS. 13-19 illustrate other forms of staple-thread units whichmay be used in accordance with the present invention.

[0054]FIG. 20 is a bottom, front and left side perspective view of oneform of a bone anchor, a staple, used with the stapler/bone anchorinserter described herein.

[0055]FIG. 21 is a front view of the stapler type bone anchor shown inFIG. 20 which can be used with the staple inserter. In this figure, oneexample of a bone anchor with an offset tip is shown, i.e. a bone anchorin which the central, longitudinal axis of the tip is offset from thecentral, longitudinal axis of the bone anchor's shaft or body. An offsettip can be provided to a staple type bone anchor or to a screw type boneanchor to protect the suture from accidentally becoming severed duringimplantation.

[0056]FIG. 22 is a front view of the curved shape that a bone anchor(e.g. that shown in FIGS. 20 or 21) can achieve after insertion intobone, a consequence of it having been formed of shape memory alloy andthe temperature of the staple having changed to its statechangingtemperature.

[0057]FIG. 23 is a perspective view of a catheter inserted into thebladder of a patient in accordance with the method of the presentinvention, with a physician's (or health care worker's) two fingerspartially inserted into a woman's vagina.

[0058]FIG. 24 is a perspective view of the hand of the physicianpressing the anterior vaginal wall of a patient against the posterior ofher pubic bone, according to the present method (with the catheter inplace).

[0059]FIG. 25 is a perspective view of the non-linear bone anchorinserter (in this case, a C-shaped inserter) inserted into the vaginalcanal, with the anchor housing pressing the anterior vaginal wall of thepatient against her pubic bone. Notice that the physician's hand, whichis used for triggering the mechanism of the inserter, is outside of thevagina and that the physician can pull the handle of the inserteragainst the resistive force of the pubic bone. An enlarged insetcross-sectional view is provided of the insertion step of the boneanchor into the pubic bone.

[0060]FIG. 26 is a perspective view of the hands of the physician tyingthe suture threads affixed to the bone anchors (the bone anchors havingfirst been implanted into the patient's pubic bone).

[0061]FIG. 27 is a perspective view, similar to that shown in FIG. 23,of an initial step in sling procedures of the present invention, inwhich a catheter is inserted into the bladder of a patient in accordancewith the method of the present invention, with a physician's (or healthcare worker's) two fingers partially inserted into a woman's vagina. Theballoon is inflated with water and located just above the bladder neck.This step is performed after a first initial step consisting of aperioperative antibiotic treatment, anaesthesia, and disinfection andcleansing of the surgical area (as are all known in the art).

[0062]FIG. 28 is a perspective view of a subsequent initial step in thesling procedures of the present invention, similar to that shown in FIG.24, in which the physician presses the anterior vaginal wall against theposterior pubic bone.

[0063]FIG. 29 is a cross sectional view of a patient, including theinserter and the phvsician's hands, showing a subsequent initial step inthe sling procedures of the present invention, in which the anchorinserter is inserted into the vagina, and the bone anchor tip isinserted through the vaginal wall into the cortex of the pubic bone(shown enlarged in the inset of the drawing).

[0064]FIG. 30 is a cross sectional view of a patient's vagina showing afirst step in the submucosal tunnel technique of the sling procedures ofthe present invention, in which a second screw is inserted on thecontralateral side of the urethral axis, which step is performed afterthe initial preparatory steps shown in FIGS. 27-29.

[0065]FIG. 31 is a cross sectional view of a patient's vagina showing asubsequent step in the submucosal tunnel technique of the slingprocedures of the present invention, in which a midline incision is cutin the anterior vaginal mucosa, just below the bladder neck.

[0066]FIG. 32 is a cross sectional view of a patient's vagina showing asubsequent step in the submucosal tunnel technique of the slingprocedures of the present invention, in which a right angle dissector ispassed submucosally from each vaginal mucosal opening to the midlineincision.

[0067]FIG. 33 is a cross sectional view of a patient's vagina showing asubsequent step in the submucosal tunnel technique of the slingprocedures of the present invention, in which the tunnels created by theanchor's sutures are dilated using a medical dilator.

[0068]FIG. 34 is a cross sectional view of a patient showing asubsequent step in the submucosal tunnel technique of the slingprocedures of the present invention, in which two sutures on one side ofthe midline incision are threaded through two holes in one side of thesling (one suture per hole), and in which the sling material is passedthrough the submucosal tunnel from one side to the other.

[0069]FIG. 35 is a cross sectional view of a patient's vagina showing asubsequent step in the submucosal tunnel technique of the slingprocedures of the present invention, in which the sling is loosely tiedto the pubic bone.

[0070]FIG. 36 is a cross sectional view of a patient's vagina showing asubsequent step in the submucosal tunnel technique of the slingprocedures of the present invention, in which the sling's tension istested, preferably using a right angle dissector, and adjusted, ifnecessary. Once the desired tension is present, sling is tightlysecured.

[0071]FIG. 37 is a cross sectional view of a patient's vagina showing asubsequent step in the submucosal tunnel technique of the slingprocedures of the present invention, in which the vaginal mucosalincisions are closed with sutures.

[0072]FIG. 38 is a cross sectional view of a patient's vagina showing afirst step in the anterior wall dissection technique of the slingprocedures of the present invention, in which a U-shaped incision ismade. The step of FIG. 38 is performed after conducting the initialsteps shown in FIGS. 27-29, the insertion of a second screw as in FIG.30, and after performing a cystoscopy to verify bladder and urethralintegrity. Once these steps are performed, a U-shaped incision is madein the vaginal mucosa, as shown in the figure, with the flap dissectedin the anterior vaginal mucosa, exposing the periurethral tissue. Anyother technique of vaginal wall dissection can also be performed.

[0073]FIG. 39 is a cross sectional view of a patient's vagina showing asubsequent step in the anterior wall dissection technique of the slingprocedures of the present invention, in which the tunnels created by theanchor's sutures are dilated.

[0074]FIG. 40 is a cross sectional view of a patient's vagina showing asubsequent step in the anterior wall dissection technique of the slingprocedures of the present invention, in which the sling is placed belowthe bladder neck, on the exposed tissue, and the sling is tied to thepubic bone surface by threading two sutures, on each side of the sling,through the two holes on that side.

[0075]FIG. 41 is a cross sectional view of a patient's vagina showing asubsequent step in the anterior wall dissection technique of the slingprocedures of the present invention, in which two sutures are tied onone side of the sling to affix the sling to the pubic bone surface, andin which, only one knot is tied on the other side, to enable fine tuningof the sling tension.

[0076]FIG. 42 is a cross sectional view of a patient's vagina showing asubsequent step in the anterior wall dissection technique of the slingprocedures of the present invention, in which the sling's tension ischecked, preferably using a right angle dissector. Once the desiredtension is present, sling is tightly secured.

[0077]FIG. 43 is a cross sectional view of a patient's vagina showing asubsequent step in the anterior wall dissection technique of the slingprocedures of the present invention, in which the vaginal muscosal flapis closed with absorbable sutures.

[0078]FIG. 44 is a cross sectional view of a patient's vagina showingthe use of a nonlinear anchor inserter, for insertion of a non-screwanchor into the public bone, in accordance with a sling procedure of thepresent invention, as disclosed herein.

[0079]FIG. 45(a) is a cross sectional view showing a sling attachedupward and forward to the mid-pubic bone, just below the Cooper'sligament. FIG. 45(b) is a further view of the sling of FIG. 45(a) shownas a view of the posterior pubic bone.

[0080]FIG. 46 is a plan view of a preferred sling design, in accordancewith the present invention.

DETAILED DESCRIPTION OF THE DRAWINGS AND THE PREFFERED EMBODIMENTS

[0081] The stapler device illustrated in FIG. 1 comprises a housing,generally designated 2, including a handle 4 which is manually grippableby the user. The illustrated stapler device may be pneumatically poweredand therefore includes a connector 6 at the bottom of the handle 4 forattaching a tube 8 connectible to a source of pressurized air. Housing 2further includes an elongated barrel 10 having a staple guide 12 at itsend for enabling the staple 14 to be ejected. Ejection of the staple 14is effected by an ejector pin 16 which is driven into sharp impactagainst the base of the staple 14 by the air pressure supplied from thepressurized air tube 8. Handle 4 includes a trigger 18 which, whendepressed, applies an air pressure pulse to ejector pin 16 to cause itto impact against the base of staple 14 and thereby to eject the stapleout through the end of guide 12. Insofar as described, such stapledevices are known, and therefore further details of its construction andoperation are not set forth.

[0082] As distinguished from the known constructions, the staple 14ejected from the guide 12 at the end of barrel 10 in FIG. 1 has a suturethread 20 secured to the staple and ejected with it. In theabove-described application, the staple is driven per vaginally into thepatient's pubic bone, and the thread 20 may then be used for securingthe bladder neck and proximal urethra.

[0083] The staple 14 in FIG. 1 is made, in one embodiment, of elasticmaterial. The staple is preferably shaped into the curved formillustrated at 14′ in FIG. 2 while it is in its “normal” condition, andis deformed into the straight form shown at 14″ in FIG. 3 while in astressed condition. It is loaded into the stapler and ejected therefromwhile in its straight stressed condition. After it has been so ejected,it returns to its curved form shown at 14″ in FIG. 2, thereby bettersecuring the staple to the bone tissue which it penetrated when it wasejected from the staple guide 12.

[0084] As shown in FIGS. 2 and 3, the staple 14 is formed with a pointedend 14 a to enable it to penetrate the bone, and with a hole 14 bapproximately midway of its length for receiving the thread 20, similarto the manner in which a thread is received in the eye of a needle.

[0085]FIGS. 4 and 5 more particularly illustrate the staple guide 12from which the staple 14, including its attached thread 20, is ejected.As shown, this guide is formed with a pair of slots 22 to accommodatethe thread 20. Thus, when the base 14 c of staple 14 is impacted by theejector pin 16, the thread 20 moves through slot 22, thereby permittingthe staple guide 12 to snugly fit around the ejected staple 14.

[0086]FIGS. 6 and 7 illustrate a modification in the construction of thestaple guide 12 in order to accommodate the thread 20 secured to thestaple 14. In the modification of FIGS. 6 and 7, the inner surface ofthe staple guide 12 is formed with a pair of recesses 22 a for receivingthe two sides of the thread 20.

[0087] The manner of using the illustrated stapler device will now bedescribed particularly with reference to FIGS. 8a-8e.

[0088] Thus, the staple 14, together with its attached thread 20, isloaded into the staple guide 12 while the staple is in its straightcondition as illustrated at 14″ in FIG. 3. Depressing trigger 18 causesa high-pressure pulse of air to be applied to ejector pin 16. This pulsecauses ejector pin 16 to impact against the end face 14 c of the staple14, thereby driving the staple into the bone as shown in FIGS. 8a and 8b. As soon as the staple penetrates the bone, it starts to return to itsnormal, curved shape as shown in FIGS. 8c and 8 d. The staple is thusfirmly anchored to the bone with its attached thread 20 extendingthrough the opening formed by the staple through the bone, as shown inFIG. 8e.

[0089] The stapler barrel 10 in FIG. 1 is preferably of a flexibleplastic tube. FIG. 9 illustrates a variation wherein the stapler barrelis in the form of a closed helical wire 110 enclosed within a thinflexible tube 111, which increases the flexibility of the barrel andthereby facilitates its placement at the proper direction. FIG. 10illustrates a variation wherein the barrel, therein designated 210, is astiff or rigid tube.

[0090]FIG. 11 illustrates a further variation wherein the stapler,therein designated 302, includes two barrels 310 a, 310 b in parallelrelation to each other to enable two staples with attached threads to beejected at the same time. In the modification illustrated in FIG. 11,each of the staple guides 321 a, 312 b receives a staple-thread unit 314a, 314 b ejected by an ejector pin 316 a, 316 b received in therespective barrel, and both ejector pins are driven at the same time byhigh pressure pulses produced upon depression of the trigger 318.

[0091] The present invention also relates to an improved inserter device(whether a stapler or screw inserter) for inserting a bone anchor(whether staple or screw) into a patient, wherein the inserter device isnon-linear. In one embodiment, the inserter is shaped in a “C” shapeddesign which allows the physician's pulling force to press the staple orscrew into the bone before and during ejection or screwing of a boneanchor. As a consequence, the physician is able to use a pulling forceagainst the resistive force of the pubic bone rather than a pushingforce against the recoil of the inserter. The device also allows thephysician to use the weight of a patient's body as counterbalancingleverage to minimize recoil of the staple during ejection of a stapleinto the patient's body. In addition, the novel geometry of the inserterallows the physician to hold the inserter and perform a per vaginalprocedure with one hand out of the vagina.

[0092] As shown in FIGS. 12a and 12 b, a stapler or bone anchor inserter810 is disclosed having a handle 815, trigger 820, anchor housing 825and an anchor shield 830. Handle 815 is attached to body 855 of the boneanchor inserter 810. Body 855 is curved such that when attached to thehandle 815 the two components form a “C” shaped apparatus. The insertercan be formed as a V-shape or another non-linear configuration.

[0093] In use, a drive pin (not shown, but located within the body)forces the anchor 835 (See FIG. 20, without suture thread shown, forease of illustration) out of anchor housing 825 and anchor shield 830(see FIG. 12a) of the stapler 810. The stapler or bone anchor inserter810 may be made of any suitable material, for example, stainless steelwhich meets surgical instrument standards. An internal spring mechanism(not shown in FIG. 12a or 12 b) is in mechanical contact with theejector pin (which is placed in contact with the bone anchor or staple).Upon the activation of the trigger 820, the ejector pin comes intocontact with the bone anchor or staple 835, providing the forcibleejecting, pushing and implanting of the bone anchor or staple 835, withattached suture thread, into bone. The ejection mechanism is activatedby the trigger 820 which can be provided with a safety release orlock-out 842 to prevent accidental, premature staple discharge.

[0094] The tail end of the anchor 835 (best seen in FIGS. 20-22) is heldin a nearly straight configuration within anchor housing 825 untilejection. The anchor housing 825 is attached to the inserter 810 priorto use, remains attached to the inserter during anchor insertion and,after insertion of the bone anchor, is disposable, with a new anchorhousing with anchor being installed onto the inserter. A retractableanchor shield 830 surrounds and protects the sharp conical front end ofthe anchor, to ease insertion. The bone anchor 835 (the specific anchor844 is shown in FIGS. 20-22) is implanted into the bone withoutpre-drilling of a hole in the patient's bone. After cocking the internalspring mechanism using a loading key 840, which is placed into androtated within loading socket 845, and attaching a bone anchor housing825 (with suture attached to anchor 835 or 844), the bone anchorinserter 810 is ready for use. The spring mechanism stores themechanical energy necessary to eject and insert the anchor into bone. Inone preferred embodiment, this is approximately 2.95 Joule±10%.

[0095]FIG. 12c illustrates a C-shaped bone anchor driver in a shapeallowing rotational insertion of a bone screw into a bone through a bodyorifice such as the vagina. The inserter consists of a handle 870 havingan internal battery 875, a battery-operated rotating motor 881, with afinger switch 880 to control operation. The motor's rotational movementis linked to a shaft adapter 883 to allow more torque with less speed ofrotation. The rotational power is transferred from the gear box throughthe inserter device to the screw adapter 890, via a flexible, rotatableshaft 895, and a flexible shaft guide 897 may be provided, as well, ifdesired.

[0096] The anchor, in this case, a screw, is connected to screw adapter890, which is at the second end of the inserter, the end opposite thehandle. The anchor or screw is disconnected from the inserter once thescrew is implanted into the bone surface. The screw protector orretractable shield 900 shields the sharp tip of the screw until it iswell positioned, so as not to accidentally damage the patient's tissue.Once the inserter is well positioned, pulling the handle 870 retractsthe spring-biased screw protector or retractable shield 900 therebyallowing the screw's sharp tip to penetrate the soft tissue. In anotherembodiment, the screw protector or retractable shield 900 may have arough edge surface, or small pins or sharp tips to hold the soft tissue(such as vaginal mucosa) and to prevent surrounding tissue rotation asthe screw rotates and penetrates the soft tissue and into the bone.Clearly, then, depressing switch 880 activates the motor 881 whichdrives the flexible shaft 895 connected to the screw adaptor 890. Thiscauses a screw (see FIGS. 12d(1)-(6)) to become embedded into the bone.

[0097]FIG. 12e shows an alternative, spring-loaded C-shaped inserter,having a different spring mechanism to that shown in FIGS. 12a & 12 c.The inserter has a dual spring mechanism which allows the user to impartmore energy and impact to the anchor during implantation into the bone.At the same time, this inserter has the significant advantage that thetwo spring design results in cancellation of the rotational movementthat the inserter may have during release. This results in a more stableanchor insertion.

[0098] This alternative inserter embodiment utilizes a hammer 1000 whichimpacts and ejects an anchor into a bone. When safety 1005 is not inplace blocking the movement of connecting cam 1010, second spring 1015can expand outward from its compressed state against second weight 1020to force second rod 1025 to the right to allow rotation of connectingcam 1010. Connecting cam 1010 is connected to both second rod 1025 andto main rod 1030. Rotation of the connecting cam 1010 in thecounterclockwise direction by second rod 1025 moving to the right, asshown in FIG. 12e, moves main rod 1030 away from its locking or “up”position against main weight 1035 which allows the spring 1040 to expandto cause hammer 1000 to impact a bone anchor.

[0099] More specifically, while main rod 1030 is forced against mainweight 1035, the hammer 1000 is maintained in a stationary position andprimed for subsequent movement to eject a bone anchor held in recess1060. Main spring 1040 is connected to main weight 1035, with mainweight 1035 slidably connected to hammer 1000. A friction disk 1045 isprovided above main spring 1040. A hammer guide 1041 is provided arounda portion of the hammer 1000, as shown in FIG. 12e. Before activation ofthe inserter, main spring 1040 is maintained in a compressed position.Movement of main rod 1030 downwardly, with main weight 1035, allows mainspring 1040 to expand outward, forcing main weight 1035 to be slammedagainst ring 1043, secured to the end of the hammer. This causes hammer1000 to rapidly move downward. The release of the energy stored in mainspring 1040 thus forces hammer 1000 downward to impact and eject a boneanchor out of recess 1060 and into a bone.

[0100] FIGS. 13-19 illustrate other constructions of staple-thread unitswhich may be used.

[0101] The unit illustrated in FIG. 13 includes a staple 114 and athread 120 similar to the construction illustrated in FIGS. 2 and 3,except that the hole 114 b through which the thread 120 is passed is atthe rear end of the staple, rather than at the middle.

[0102]FIG. 14 illustrates a construction wherein the staple 214 isprovided with a bore 214b extending at an angle to the longitudinal axisof the staple 214 with the end of the thread 220 received and fixedtherein by crimping the staple. FIG. 15 illustrates a constructionwherein the bore 314 b is in the base 314 c of staple 314 and extendsalong or parallel to the longitudinal axis of the staple 314, the thread320 being received within the bore 314 b and fixed therein by crimpingthe staple. FIG. 16 illustrates a construction similar to that of FIG.15, except that part of the base 414 c of the staple 414, formed withthe axial bore 414 b for receiving the thread 420, is cut away so thatthe impact of the ejector pin against the base of the staple will notimpact against the end of the thread.

[0103]FIG. 17 illustrates a further variation wherein the staple 514 isformed with a plurality of barbs 515 projecting from its outer surface,to fix the staple to the bone into which it has penetrated. The thread520 is passed through a hole 514 b in the staple.

[0104]FIG. 18 illustrates a staple made of bent wire. FIG. 19illustrates a staple with a split tail 714 c, which is straightenedunder stress when first inserted into the staple guide 12 and splitsafter ejection, a consequence of its shape memory.

[0105] In one recommended embodiment, the bone anchor can be made of asingle piece of a shape memory alloy, such as the nickel-titanium alloycalled Nitinol. One form of bone anchor, for example, which can be usedwith the present invention, has a conical front end 846 (See FIGS.20-22) with diameters ranging from 1.9-2.4 mm, and a tail end with anearly rectangular cross-section. The tail portion is preferably 6.0 mmlong with a width that ranges from 1.9-2.4 mm and a thickness of about0.6 mm. The anchor tail 844 contains two holes 848 and 850 which areused for threading the suture. An example of a suture thread which canbe used in the bone anchor is sterile polypropelene monofilament No. 1.The bone anchor is depicted in FIGS. 20 through 22. According to thepreferred embodiment of the bone anchor 835, the longitudinal axis ofthe tail end is offset from the center axis of the conical tip 846. Thisis best seen in FIGS. 21 and 22.

[0106] Within the bone medulla, the bone anchor 835 soon heats to bodytemperature, changing by the characteristics of shape memory alloy, forexample, from a straight to a curved shape, i.e., the longitudinal axisof the anchor changes, after insertion. This is shown in FIG. 22.According to one preferred embodiment, the end of the tail and the rearend of the conical tip, after heating of the bone anchor sufficient tochange its shape, will subtend an angle of about 75° ±16° (as seen inFIG. 22). This change of shape is because of the fabrication of theanchor from shape memory alloy. This curved shape facilitates fixationof the anchor within the bone and inhibits the inadvertent removal ofthe anchor. Pulling on the suture, which is connected to the anchor 835,causes the anchor to rotate within the bone and further fixate in thebone. The reformation of the anchor to its curved shape (the shape ithad prior to straightening by being held in the anchor housing 835) androtation, together, prevent the anchor from inadvertently exitin,,through the entrance path provided into the bone. The small profile andsharpness of the anchor tip 846 allow easy insertion into the bone withminimal damage to the bone surface.

[0107] Thus, the present invention provides an apparatus and methodwhich (in the anchor ejection or screwing mode) does not requirepre-drilling of the bone or soft tissue dissection to insert the boneanchor into the bone. Similarly, the bone anchor does not require cementor other fixative to remain in place.

[0108] The bone anchor and bone anchor inserter are supplied sterile. Asthe bone anchor inserter is a multiple use device, the inserter (and itsloading key) should, of course, be cleaned and sterilized before eachnew patient procedure. Cleaning is accomplished by washing and rinsingthe inserter and loading key with water and a liquid detergent, whilescrubbing with a flexible brush to completely remove all traces ofblood. The inserter and loading key should be rinsed thoroughly withwater to remove detergent residues. Panels in the inserter body allowaccess for cleaning. Once cleaned, the inserter and loading key may becloth or air dried. The inserter and loading key may be sterilized byheat or steam autoclave, or gas EtO), in accordance with hospitalprocedures for sterilization of stainless steel surgical instruments.

[0109] Various different types of bone screws 920 can be used inaccordance with the present invention. As shown in FIG. 12d(1), a bonescrew is disclosed having a conical tip 910 and a screw body 915. Thediameter of each of the screw threads 928 (the grooves, recesses orindentations in the material of the screw) is constant along the screwbody. The suture 925 is attached at a hole in the end 927 of the bonescrew.

[0110]FIG. 12d(2) shows a bone screw 920 with a more tapered conical tip930 and a screw body 935. In this version, the diameter of the screwthreads 940 vary. The diameters of the screw threads 940 increase fromsmall diameters near the apex of the conical tip to greater diametersnear the screw body 935. The screw threads 940 can be located on all ora portion of the screw body as well, if desired. The suture 950 isattached through a hole in the end 947 of the screw.

[0111]FIG. 12d(3) is similar to FIG. 12d(1). In this figure, however,the suture is shown attached through a hole in the middle 952 of thebone screw.

[0112]FIG. 12d(4) shows a bone screw 920 in which the screw threads orgrooves are formed by wrapping spring wire 956 around a solid body. Thebody has a leading tip 970 and a shaft 972, of smaller relative crosssection. A trailing end 974 with a hole is provided for attaching thesuture thread 976. The spring wire is wrapped on the shaft 972 andmaintained between leading tip 970 and the trailing end 974.

[0113]FIG. 12d(5) shows a bone screw similar to that in FIG. 1d(4). Inthis screw, leaf springs 958 are provided. Leaf springs 958 areinitially flattened against the side surface of the bone screw, i.e.,when the screw is inserted into the bone. Upon insertion, however, theleaf springs 958 expand outward from a compressed to a non-compressedstate (due to the elasticity which is characteristic of a spring) toprovide greater anchoring of the bone screw within the bone.

[0114]FIG. 12d(6) discloses a bone screw in which the screw threads orgrooves are formed by wrapping a spring plate 963 around the screw bodyor shaft of the screw. Here, too, the spring plate is held between theleading tip and the trailing end.

[0115] The bone screw is typically made of a medical grade alloy such asStainless Steel 316. Its sharp tip and small diameter allows for itspenetration through the vaginal wall and the periosteum, withoutpre-drilling a hole. As the screw is rotated by the inserter, which maybe linear, C- or V-shaped, it further enters the bone until it reaches aprescribed depth within the bone. The screw then automaticallydisconnects from the rotating inserter shaft. The medical technique ofinserting a bone screw into the pubic bone through the vagina for thepurposes of bladder neck suspension is also within the scope of thepresent invention, as is the bone screw inserter.

[0116] While the invention has been described with respect to oneparticular application, it will be appreciated that the described anchordevice and anchor-thread units may be used for other applications, e.g.,for shoulder dislocations, endoscopic operations, or the like. Theanchor inserter may also be electrically operated and may use othermechanical impact or screw-type devices for driving the anchor. Theanchors themselves may be of known bio-absorbable materials.

[0117] Following is one procedure for performing the above-describedoperation: A 20F urethral catheter is inserted into the bladder, and aballoon is inflated to 20 cc and retracted gently downwardly against thebladder neck. The surgeon inserts two fingers into the vagina, pressingthe anterior vaginal wall with one finger on each side of the urethra,which is felt because of the inserted catheter. By pressing the fingersupwardly and backwardly, the bladder neck and proximal urethra arepressed against the posterior wall of the pubic bone. At this stage, twostaples are ejected longitudinally on each side of the urethra, about1-2 cm apart. The two threads on each side of the urethra are tied oneto the the other. They may be tied on the vaginal mucosa, in which casethe tension will embed the threads to the sub-mucosa after some time.Alternatively, the threads may be tied under the vaginal mucosa bypassing one of the threads on the same side. The threads may be made ofa monofilament non-absorbent material, as well as of an absorbentmaterial, dependent on the preference of the physician.

[0118] Further methods of the present invention is shown in FIGS. 23-26.With the patient in lithotomy position, the surgical area and the vaginaare cleaned and disinfected. A Foley catheter is inserted inside thebladder, and the balloon is inflated with approximately 1020 cc ofwater. The catheter is then pulled backwardly to locate the balloon justabove the bladder neck as shown in FIG. 23.

[0119] The catheter (within the urethra) and the balloon at the bladderneck are palpated by the physician's finger tips. Pressing the fingersupward and forward, the anterior vaginal wall is pressed against theposterior pubic bone surface, as shown in FIG. 24.

[0120] The bone anchor inserter (whether a stapler/impact or ascrewdriver-type inserter) is then inserted into the vagina (see FIG.25) near the bladder neck and approximately 2 cm. to the side of theurethra. The inserter is pulled against the pubic bone. Notice that thetriggering hand of the physician is external to the vagina and that theforce applied by the physician is one of pulling against the resistiveforce of the pubic bone. The tip of the bone anchor 835 touches andpenetrates the vaginal wall and enters the cortex of the pubic bone.

[0121] Thus, once the inserter is stable and properly positioned in thevagina, the trigger 820 (or switch 880, for the screw inserter) ispulled and the bone anchor 835 penetrates and fixates within the bone.When the end of the inserter 810 is under the pubic bone, and pressedagainst it, the physician pulls up on the handle 815 of the stapler orbone anchor inserter 810. By doing so, the physician lifts the anchor835 or screw 920 and anchor housing 825 or screw adaptor 890 against thepubic bone. A portion of the weight of the patient resists the liftingof the inserter, pressing against it firmly. As a result, the lifting ofthe stapler or bone anchor inserter 810 is performed against some of theweight of the patient, ensuring a firm and effective contact of theanchor tip with the pubic bone. Mechanically, it is easier for thephysician to pull on the inserter with his or her hand outside of thevagina than for the physician to have his or her triggering hand withinthe vagina and pushing the inserter against the pubic bone. Thepenetration of the tip of the bone anchor into the bone cortex beforeejection or screwing further increases the stability of the ejectioninto the pubic bone. The use of the non-linear or C-shaped inserterallows at least part of the patient's weight to counterbalance therecoil of the spring mechanism. The patient's body weight, along withthe inserter's shape, provides the physician with suitable leverage forensuring penetration of the anchor 835 or screw 920 into the pubic bone.This is especially important in the use of the present bone anchordevice which, in the case of the ejected anchor, seeks to avoidpre-drilling of a hole, followed by anchor insertion.

[0122] Releasing the safety 842 first and then pressing the trigger 820of the device activates the inserter spring mechanism (not shown) whichejects the anchor 835 to a prescribed depth within the bone (e.g. 2.5mm) so that no portion of the anchor protrudes from the bone surface.Although the end of the inserter will experience a reaction force whenthe staple is ejected, the weight of the patient, pressing downwardagainst the inserter end (anchor housing 825 and anchor shield 830)combined with the force exerted by the physician by pulling the handle815 of the bone anchor inserter 810 upward (so that the end of theinserter is forced against the weight of the patient and the penetrationof the tip of the anchor into the pubic bone before ejection) result ina firm and solid contact between the inserter and the pubic bone duringand through the insertion process, minimizing any problems of insertionassociated with stapler recoil.

[0123] Two to four anchors are preferably inserted into the patient.Bone anchors are inserted on each side of the urethral axis or parallelalong each side of the posterior aspect of the superior pubic boneramus, lateral to the symphysis pubis. When four bone anchors are used,two bone anchors are inserted on each side of the urethral axis orparallel along each side of the posterior aspect of the superior pubicramus, about 2 cm. lateral to the symphysis pubis. Each pair of two boneanchors is inserted with the two bone anchors in a pair approximately 2cm. apart. Cystoscopy is then performed to verify that there are nobladder or urethral perforations.

[0124] The suture threads extending from the anchors are then tied. Forexample, when inserting four bone anchors, four sets of suture threadsshould protrude from the vaginal wall. The suture threads are tied fromone bone anchor to the other, ipsilaterally on each side of the urethra,as shown in FIG. 26. They may be tied either above the vaginal mucosa orbelow the vaginal mucosa (using a deshamp) with or without vaginaldissection. The tie may be left as is or pushed beneath the mucosa.

[0125] Suprapubic or Foley urethral catheterization is then performed.The suprapubic catheter is to remain until complete bladder emptying isachieved by normal urination. Prophylactic antibiotic is administeredperioperatively. Physical strain and lifting by the patient is to beavoided for approximately 2-3 months.

[0126] In cases where the urethra itself is very wide, the threads maybe used for engaging and elevating the urethra to the posterior pubicbone as in a “sling operation”.

[0127] Numerous different types of sling procedures can be provided, inaccordance with the invention. These sling procedures are preferablyprovided for the treatment of urinary stress incontinence as disclosedabove and herein. Alternatively, it is contemplated that they may bealso useful in other medical procedures to correct other anatomicpathologies and/or relieve discomforts of a patient.

[0128] In the preferred embodiment of the invention, the sling procedureis a pervaginal procedure in which one or more bone anchors are insertedthrough the vaginal wall of the patient to enter the pubic bone, and inwhich suture thread and a sling are utilized to adjust the anatomicposition of the bladder neck and the urethra of the patient, or morespecifically, to suspend the bladder neck. The bone anchors may be bonescrews and/or bone staples, and preferably have the suture suture threadalready attached thereto before they are inserted into the vagina of thepatient. In a further preferred embodiment of the invention, insertionof the anchors is conducted using a nonlinear inserter, preferably oneof the inserters disclosed herein.

[0129] In a preferred embodiment, the In-Fast™ Bone Screw System and/orthe In-Tac™ Bone Anchor System is used, both of which are available fromInfluence, Inc. of San Francisco, Calif.

[0130] In accordance with the various embodiments of the sling procedureof the present invention, the procedure is initiated by a pervaginalinsertion of an anchor into the patient. After a perioperativeantibiotic treatment, the patient is placed under spinal, general orlocal anesthesia and in the lithotomy position, and the surgical areaand the vagina are cleaned and disinfected. A Foley catheter 706 is theninserted inside the bladder 710, and the balloon 712 is inflated withapproximately 10-20 cc of water. The catheter 706 is then gently pulledto locate the balloon 712 just above the bladder neck 716 as shown inFIG. 27.

[0131] When the balloon 712 has been positioned, the catheter 706 isthen located, within the urethra, between the physician's index andsecond fingers so that the finger tips are touching the balloon at thebladder neck. The physician then, by pushing his or her fingers upwardand forward, presses the anterior vaginal wall against the posterior ofthe pubic bone 718, as shown in FIG. 28.

[0132] As shown in FIG. 29, after pressing the anterior vaginal wall 724against the pubic bone, and while still feeling the catheter within theurethra, the physician then inserts the bone anchor insertion device 722(preferably a nonlinear bone screw inserter) into the vagina, below thebladder neck and lateral to the symphysis pubis, about 2 cm. to the sideof the urethra. The inserter device 722 is then pulled upward until thescrew 726 presses the anterior vaginal wall 724 against the pubic bone718.

[0133] In the preferred embodiment, an inserter 722 is used having aretractable shield 730. Retractable shield 730 is a protective cover forthe screw 726 which is designed such that the application of pressure tothe shield 730 causes the shield to retract and reveal the screw. Forexample, the shield 730 can be flexible, such that it bends, contracts,or compresses when force is provided to it. Or, the shield 730 can reston springs while the screw does not, so that application of pressure tothe shield retracts it, while the screw remains in place.

[0134] Once the shield 730 is pressed against the pubic bone 718, thescrew shield 730 will collapse and the tip of the bone screw 726 willbecome exposed so as to allow it to penetrate the vaginal wall 724 andenter the cortex of the pubic bone 718, as shown in FIG. 29. The safetylock of the inserter 722 can then be released to allow deeper insertionof the screw 726 into the bone, by continuously pressing the inserter'soperate button to insert the screw. When the screw 726 has been totallyinserted (after approximately 10-20 seconds, as indicated by change inthe inserter's motor tone and cessation of twisting of protrudingsuture), as shown in the exploded view of FIG. 29, the operate button isreleased and the inserter can be removed from the vagina for reloading.

[0135] Once the first anchor (preferably a screw) has been inserted intoa patient, various embodiments are available for the methods of theinvention. In accordance with the invention, a submucosal tunneltechnique or an anterior wall dissection technique can preferably beperformed, as disclosed below.

Submucosal Tunnel Technique

[0136] In accordance with the submucosal tunnel technique, once thefirst screw 726 has been inserted, a second screw 736 is inserted in thesame elevation as in the first, on the contralateral side of theurethral axis, as shown in FIG. 30. When the second screw 736 is inplace, a cystoscopy is performed to verify bladder and urethralintegrity. A midline incision 740 (see FIG. 31) about 1.5-2 cm long isthen cut in the anterior vaginal mucosa, just below the bladder neck 716as shown in FIG. 31.

[0137] A right angle dissector 744 is then passed submucosally from eachvaginal mucosal opening to the midline incision 740 to create asubmucosal tunnel 748 just below the bladder neck 716, as shown in FIG.32.

[0138] The tunnels created by the anchor's sutures are then dilated.Dilation is performed by threading one pair of sutures through the tipof a dilator 750. The dilator 750 is inserted into the vagina and, whilepulling on the sutures, it is advanced and pushed up along the sutures,perpendicular to the pubic bone surface, as shown in FIG. 33. Once thedilator 750 touches the bone cortex, the dilator is then openedapproximately 5 mm and pulled back, and out of the patient, in the openposition. This procedure is then repeated for the contralateral pair ofsutures.

[0139] Once the tunnels created by the sutures have been dilated, thesling is introduced into the vagina. As shown in FIG. 34, the twosutures 728 on one side are threaded through the two holes in one sideof the sling 752. The sling material 752 is then passed through thesubmucosal tunnel from one side to the other.

[0140] As shown in FIG. 35, when the sling 752 has been advanced acrossthe tunnel, two sutures on one side are tied towards the pubic bone toaffix the sling to the pubic bone surface. On the other side, only asingle knot is tied to enable fine tuning of the sling tension, ifrequired.

[0141] To check the sling's tension, a right angle clamp 758 is insertedthrough the midline incision 740 above the sling material 752 and usedto pull the sling material downwards gently, as shown in FIG. 36. Thesling 752 should be loose enough to permit approximately 0.5 cm of slingmovement. If the sling is too tight or too loose, the sling tension isadjusted (by adjusting the tension on the side with the single knot),and then, once sufficient tension has been achieved, that side of thesling is secured. The vaginal mucosal incisions are then closed withabsorbable sutures as shown in FIG. 37.

[0142] A suprapubic or urethral catheterization is then performed. Thedraining catheter should remain until complete bladder emptying isachieved by normal urination, normally between 1 to 2 days. Prophylacticantibiotics should be administered perioperatively for approximately 5days after the procedure, and physical strain and lifting by the patientshould be avoided for 2-3 months. In addition, it is recommended thatthe lot numbers of the screws used in the procedure should be recordedon the patient's chart. Upon completion of the procedure, the inserter,if of a disposable nature (not reusable) can be discarded.

Anterior Wall Dissection Technique

[0143] In an alternate embodiment of the sling procedure of the presentinvention, an anterior wall dissection technique is provided. Inaccordance with this embodiment, the initial steps described above withrespect to the submucosal tunnel technique are performed, from theantibiotic treatment through the insertion of the second screw on thecontralateral side and the performance of a cystoscopy to verify bladderand urethral integrity, as disclosed above, and shown in FIGS. 27-30.

[0144] Following the cystoscopy, a U or other incision is made in thevaginal mucosa. The flap is dissected in the anterior vaginal mucosa,exposing the periurethral tissue as shown in FIG. 38.

[0145] The tunnels created by the anchor's sutures are then dilated, asshown in FIG. 39. This is performed by threading one pair of suturesthrough the tip of a dilator. The suture is then held, under tension,and the dilator is pushed up along the sutures, perpendicular to thepubic bone surface. Once the dilator touches the bone cortex, thedilator is opened approximately 5mrn and pulled back, and out of thepatient, in the open position. This procedure is then repeated for thecontralateral pair of sutures.

[0146] The sling is then placed below the bladder neck, on the exposedtissue. On each side of the sling, two sutures are threaded through thetwo holes in the sling on that side, a suture through each hole, asshown in FIG. 40. On one side, two sutures are tied toward the pubicbone to affix the sling to the pubic bone surface. On the other side,only one L-not is tied so as to enable fine tuning of the sling tensionif required, as with the submucosal tunnel technique, and as shown inFIG. 41.

[0147] To check the sling's tension, a right angle clamp is placed abovethe sling material and pulled downwards gently, as shown in FIG. 42. Thesling should be loose enough to permit up to 0.5 cm of sling movement.The vaginal mucosal flap is then closed with absorbable sutures, asshown in FIG. 43.

[0148] A suprapubic or urethral catheterization is then performed. Thedraining catheter should remain until complete bladder emptying isachieved by normal urination, normally between 1 to 2 days. Prophylacticantibiotics should be administered perioperatively for approximately 5days after the procedure, and physical strain and lifting bythe patientshould be avoided for 2-3 months. In addition, it is recommended thatthe lot numbers of the screws used in the procedure should be recordedon the patient's chart. Upon completion of the procedure, the insertercan be discarded.

Non-Screw Bone Anchor Techniques

[0149] In alternate embodiments of the invention, the Submucosal TunnelTechnique and the Anaterior Wall Dissection can be performed with anon-screw bone anchor. In the preferred embodiment, such insertions areperformed using the In-Tac™ Bone Anchor System, available fromInfluence, Inc. of San Francisco, Calif.

[0150] In these embodiments, the procedure is also conducted using apervaginal insertion of an anchor into the patient. After aperioperative antibiotic treatment, the patient is placed under spinal,general or local anesthesia and in the lithotomy position, and thesurgical area and the vagina are cleaned and disinfected.

[0151] The anchor inserter is then loaded with an anchor. Initially, theloading key is placed into its key hole on the inserter and the key isturned clockwise approximately one half turn until the loading key willnot turn further. The first anchor is then placed within the anchorinserter.

[0152] A Foley catheter is then inserted inside the bladder, and theballoon is inflated with approximately 10-20 cc of water, as previouslydescribed. The catheter is then gently pulled to locate the balloon justabove the bladder neck, as shown in FIG. 27.

[0153] When the balloon 712 has been positioned, the catheter 706 isthen located, within the urethra, between the physician's index andsecond fingers so that the finger tips are touching the balloon at thebladder neck. The physician then, by pushing his or her fingers upwardand forward, presses the anterior vaginal wall against the posterior ofthe pubic bone 718, as shown in FIG. 28.

[0154] As shown in FIG. 44, while stil feeling the catheter within theurethra, the bone anchor inserter is inserted into the vagina, below thebladder neck, lateral to the symphysis pubis, about 2 cm. to the side ofthe urethra, and pulled upward until the anchor housing is pressing theanterior vaginal wall against the pubic bone. The anchor shield willthen retract or collapse and the tip of the bone anchor should beexposed to enable it to penetrate the vaginal wall and enter the cortexof the pubic bone, as also shown in FIG. 44.

[0155] The safety lock of the inserter is then released, and thephysician pulls upwards on the handle of the inserter until an anchor isdeployed. Preferably, the safety lock will not allow anchor deploymentunless sufficient pressure is applied to the inserter handle. Thephysician can then continue with either the Submucosal Tunnel Techniqueor the Anterior Wall Dissection technique, as described above.

[0156] A further embodiment of the invention in which the sling materialis pervaginally suspended from the pubic bone is shown in FIGS. 45(a)and (b). FIG. 45(a) shows a sling material wherein the sling is attachedupward and forward to the mid-pubic bone, just below the Cooper'slgament. A triangle is formed by the sling material and the natural “V”of the pubic bone, providing a “free space” for the urethra which mayreduce the tendency for overcorrection. FIG. 45 (b) illustrates thesling of FIG. 45(a), taken as a view of the posterior pubic bone. Inthese embodiments, the sling material is positioned as a hammock below aportion of the female anatomy (i.e. the bladder neck and/or theurethra), the sling being suspended to the posterior surface of thepubic bone by a pervaginal technique, and with the bone anchors likewisebeing inserted pervaginally. In the preferred embodiment of theinvention of FIG. 45, the sling is directly attached to the pubic bonewithout the use of intervening sutures, preferably by inserting a boneanchor through the sling material to directly attach the sling to thepubic bone. in accordance with the inventions of the presentapplication, one preferred sling design is shown in FIG. 46. This slingis preferably a biocompatible texturized fabric impregnated with anabsorbable gelatin. It is preferred that a soft pliable material with amatrix that facilitates tissue ingrowth be used. The material can beformed with a warp knitting process. Gelatin impregnation is preferablycrosslinked to a set level to control the resorption rate and reduce thepotential for inflammation. The sling is also preferably prepunctured tofacilitate the threading of suture or insertion of a bone anchortherethrough. In one preferred embodiment, the sling is approximately5.5 cm in length and approximately 2 cm in width at its widest portion.

[0157] Having described this invention with regard to specificembodiments, it is to be understood that the description is not meant asa limitation since further variations or modifications may be apparentor may suggest themselves to those skilled in the art. It is intendedthat the present application cover such variations and modifications asfall within the scope of the appended claims.

We claim:
 1. A method of treating a female patient for urinary stressincontinence, comprising: per vaginally inserting a bone anchor to enterthe posterior wall of the pubic bone, said bone anchor comprising suturethread secured thereto; and, using said surture thread and a sling totreat the incontinence.
 2. A method as claimed in claim 1, wherein saidsuture thread and said sling are used to position the bladder neck ofthe patient.
 3. A method as claimed in claim 1, wherein said suturethread and said sling are used to position the urethra of the patient.4. A method as claimed in claim 1, wherein said suture thread and saidsling are used to positon the bladder neck and the urethra of thepatient.